Skip to main content

Cysteine-rich with EGF-like domains 2 (CRELD2) is an endoplasmic reticulum stress-inducible angiogenic growth factor promoting ischemic heart repair.

Nature cardiovascular research

Authors: Xuekun Wu, Linqun Zheng, Marc R Reboll, Lillian F Hyde, Elvira Mass, Hans W Niessen, Maike Kosanke, Andreas Pich, Evangelos Giannitsis, Jochen Tillmanns, Johann Bauersachs, Joerg Heineke, Yong Wang, Mortimer Korf-Klingebiel, Felix Polten, Kai C Wollert

Tissue repair after myocardial infarction (MI) is guided by autocrine and paracrine-acting proteins. Deciphering these signals and their upstream triggers is essential when considering infarct healing as a therapeutic target. Here we perform a bioinformatic secretome analysis in mouse cardiac endothelial cells and identify cysteine-rich with EGF-like domains 2 (CRELD2), an endoplasmic reticulum stress-inducible protein with poorly characterized function. CRELD2 was abundantly expressed and secreted in the heart after MI in mice and patients. Creld2-deficient mice and wild-type mice treated with a CRELD2-neutralizing antibody showed impaired de novo microvessel formation in the infarct border zone and developed severe postinfarction heart failure. CRELD2 protein therapy, conversely, improved heart function after MI. Exposing human coronary artery endothelial cells to recombinant CRELD2 induced angiogenesis, associated with a distinct phosphoproteome signature. These findings identify CRELD2 as an angiogenic growth factor and unravel a link between endoplasmic reticulum stress and ischemic tissue repair.

© 2024. The Author(s).

PMID: 39196188

Participating cluster members